Julia Lackenby

ORCID: 0000-0003-0933-3998
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About
Contact & Profiles
Research Areas
  • SARS-CoV-2 and COVID-19 Research
  • Animal Virus Infections Studies
  • Parasitic infections in humans and animals
  • Bacterial Infections and Vaccines
  • Immunotherapy and Immune Responses
  • T-cell and Retrovirus Studies
  • Viral gastroenteritis research and epidemiology
  • Congenital Anomalies and Fetal Surgery
  • Parasitic Infections and Diagnostics
  • COVID-19 Clinical Research Studies
  • Animal Disease Management and Epidemiology
  • Leech Biology and Applications
  • Urological Disorders and Treatments
  • Virology and Viral Diseases
  • Parasites and Host Interactions
  • Parasite Biology and Host Interactions
  • interferon and immune responses
  • Helminth infection and control
  • vaccines and immunoinformatics approaches
  • Influenza Virus Research Studies

The University of Queensland
2020-2024

The University of Melbourne
2010-2012

The University of Adelaide
2007

Efforts to develop and deploy effective vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continue at pace. Here, we describe rational antigen design through manufacturability vaccine efficacy of a prefusion-stabilised spike (S) protein, Sclamp, in combination with the licensed adjuvant MF59 'MF59C.1' (Seqirus, Parkville, Australia).A panel recombinant Sclamp proteins were produced Chinese hamster ovary screened vitro select lead candidate. The structure this was...

10.1002/cti2.1269 article EN cc-by-nc-nd Clinical & Translational Immunology 2021-01-01

Recombinant antigens from the oncosphere stage of parasite Taenia solium were expressed in Escherichia coli. The TSOL16, TSOL45-1A and TSOL45-1B recombinant antigens, each consisting fibronectin type III (FnIII) domain S, produced as fusion proteins with glutathione S-transferase (GST) maltose binding protein (MBP). Groups pigs immunized twice GST fusions boosted a third time MBP prior to receiving challenge infection T. eggs. TSOL16 antigen was found be capable inducing high levels immunity...

10.1016/j.vaccine.2012.04.019 article EN cc-by Vaccine 2012-04-19

Abstract The human T-lymphotropic virus type 1 (HTLV-1) infects millions of people globally and is endemic to various resource-limited regions. Infections persist for life are associated with increased susceptibility opportunistic infections severe diseases including adult T cell leukemia/lymphoma HTLV-1-associated myelopathy-tropical spastic paraparesis. No HTLV-1-specific anti-retrovirals have been developed it unclear whether existing treatment immunodeficiency (HIV) efficacy against...

10.1186/s12985-024-02288-z article EN cc-by Virology Journal 2024-01-10

DAO Diseases of Aquatic Organisms Contact the journal Facebook Twitter RSS Mailing List Subscribe to our mailing list via Mailchimp HomeLatest VolumeAbout JournalEditorsSpecials 74:235-242 (2007) - doi:10.3354/dao074235 Effect water temperature on reproductive development Benedenia seriolae (Monogenea: Capsalidae) from Seriola lalandi in Australia Julia A. Lackenby1,3,*, Clinton B. Chambers1,4, Ingo Ernst1,5, Ian D. Whittington1,2 1School Earth and Environmental Sciences, Darling Building...

10.3354/dao074235 article EN Diseases of Aquatic Organisms 2007-03-13

Abstract Efforts to develop and deploy effective vaccines against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) continue at pace with more than 30 candidate now in clinical evaluation. Here we describe the preclinical development of an adjuvanted, prefusion-stabilised Spike (S) protein “Sclamp” subunit vaccine, from rational antigen design through assessing manufacturability vaccine efficacy. In mice, elicits high levels neutralising antibodies epitopes both within outside...

10.21203/rs.3.rs-68892/v1 preprint EN cc-by Research Square (Research Square) 2020-10-01

Prior to 2020, the threat of a novel viral pandemic was omnipresent but largely ignored. Just twelve months prior Coronavirus disease (COVID-19) our team received funding from Coalition for Epidemic Preparedness Innovations (CEPI) establish and validate rapid response pipeline subunit vaccine development based on proprietary Molecular Clamp platform. Throughout course 2019 we conducted two mock tests system antigen production against potential, emerging pathogens, Achimota paramyxovirus...

10.3389/fimmu.2020.592370 article EN cc-by Frontiers in Immunology 2020-11-04

Immunohistochemistry and immunofluorescence with confocal microscopy were used to localize the host-protective antigens of Taenia saginata (TSA9 TSA18) solium (TSOL16, TSOL18 TSOL45). In nonactivated oncospheres, TSA9 TSOL45 found primarily in cytoplasm penetration gland type one (PG1) cell. A similar pattern staining was seen for oncospheres T. that remained within oncospheral membrane. addition, there less intense quadri-nucleate 2 (PG2) TSA18, TSOL16 predominantly PG2 activated had...

10.1111/j.1365-3024.2010.01230.x article EN Parasite Immunology 2010-05-14

We previously demonstrated the safety and immunogenicity of an MF59-adjuvanted COVID-19 vaccine based on SARS-CoV-2 spike glycoprotein stabilised in a pre-fusion conformation by molecular clamp using HIV-1 41 sequences. Here, we describe 12-month results adults aged 18-55 years ≥56 years.Phase 1, double-blind, placebo-controlled trial conducted Australia (July 2020-December 2021; ClinicalTrials.govNCT04495933; active, not recruiting). Healthy (Part 1: years; Part 2: years) received two doses...

10.1016/j.ebiom.2023.104842 article EN cc-by-nc-nd EBioMedicine 2023-10-20

Abstract The human T-lymphotropic virus type 1 (HTLV-1) infects millions of people globally and is endemic to various resource-limited regions. Infections persist for life are associated with increased susceptibility opportunistic infections severe diseases including adult T cell leukemia/lymphoma (ATLL) HTLV-1-associated myelopathy-tropical spastic paraparesis (HAM-TSP). No HTLV-1-specific anti-retrovirals have been developed it unclear whether existing treatment immunodeficiency (HIV)...

10.1101/2023.05.25.542289 preprint EN cc-by-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-05-25

Background: We assessed the safety and immunogenicity of an MF59-adjuvanted subunit vaccine for COVID-19 based on recombinant SARS-CoV-2 spike glycoprotein stabilised in a prefusion conformation by novel molecular clamp (Sclamp).Methods: Phase 1, double-blind, placebo-controlled trial conducted Australia (July 2020–ongoing; ClinicalTrials.gov NCT04495933). Healthy adults (18-55 years) received two doses placebo, 5-μg, 15-μg, or 45-μg Sclamp, one dose Sclamp followed 28 days apart (n=120; 24...

10.2139/ssrn.3769210 article EN SSRN Electronic Journal 2021-01-01

Efforts to develop and deploy effective vaccines against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) continue at pace. Here we describe rational antigen design through manufacturability vaccine efficacy, of a prefusion-stabilised Spike (S) protein, Sclamp. This strategy uses an orthogonal stabilisation approach compared canonical vaccines, in combination with the licensed adjuvant MF59 (Seqirus). In mice, Sclamp elicits high levels neutralising antibodies, as well broadly...

10.2139/ssrn.3736395 article EN SSRN Electronic Journal 2020-01-01

Background: We previously demonstrated the safety and immunogenicity of an MF59-adjuvanted COVID-19 vaccine based on SARS-CoV-2 spike glycoprotein stabilised in a pre-fusion conformation by molecular clamp using HIV-1 41 sequences. Here, we describe 12-month results adults aged 18–55 years ≥56 years.Methods: Phase 1, double-blind, placebo-controlled trial conducted Australia (July 2020–December 2021; ClinicalTrials.gov NCT04495933; active, not recruiting). Healthy (Part 1: years; Part 2:...

10.2139/ssrn.4401687 preprint EN 2023-01-01
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